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Advances and Perspectives in Genetics of Congenital Thyroid Disorders Associated with Thyroglobulin Gene Mutations

<p>Dyshormonogenesis due to thyroglobulin (TG) gene mutations is a rare cause of congenital hypothyroidism with an estimated incidence of approximately 1 in 100,000 newborns. The TG gene is organized in 48 exons, spanning over 270 kb on human chromosome 8q24. The human TG mRNA is 8.5 Kb long a...

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Xehetasun bibliografikoak
Egile Nagusiak:	Héctor M.Targovnik (Egilea), Cintia E.Citterio (Egilea), Sofi a Siffo (Egilea), Carina M.Rivolta (Egilea)
Formatua:	Liburua
Argitaratua:	Open Journal of Biological Sciences - Peertechz Publications, 2016-12-19.
Gaiak:	Review Article
Sarrera elektronikoa:	Connect to this object online.
Etiketak:	Etiketa erantsi Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

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